Pharmaceutical Analysis Service

Navigate Pharmaceutical Success: Trust CD BioGlyco's Precision Analysis Solutions!

In the progression of pharmaceutical development, pharmaceutical analysis has played a vital role. To assist researchers in exploring the field of pharmaceuticals, CD BioGlyco offers an important service, Pharmaceutical and Biological Analysis Service, which is a specific aspect of pharmaceutical and Biological Product development. Our service involves the application of analytical techniques to evaluate the quality, safety, and efficacy of drugs at various stages of the development process, including drug discovery, formulation, and manufacturing. Our comprehensive analysis services are specifically designed to cater to the intricate analysis requirements of pharmaceuticals that are either based on carbohydrates or incorporate carbohydrates into their composition.

We employ advanced techniques and methodologies to evaluate the properties, structure, and potency of these drugs, ensuring accurate and insightful analysis results, including titrimetry, spectrometry, chromatography, and capillary electrophoresis, the electro analytical methods. They are vital in comprehending the drug's physical and chemical stability, influencing the selection and design of dosage forms, evaluating the stability of drug molecules, quantifying impurities, identifying impurities above established thresholds, assessing the toxicity profiles of these impurities compared to the active pharmaceutical ingredient (API), when applicable, and determining the drug content in marketed products.

Our pharmaceutical analysis involves the study of analytical methods and techniques related to pharmaceuticals. Here are some key components of our pharmaceutical analysis:

Fig.1 Pharmaceutical Analysis Service at CD BioGlyco. (CD BioGlyco)

• Identity: Based on examining their composition, structure, and properties, we conduct identification tests by employing chemical, physical, and biochemical techniques. These methods are used to determine the authenticity of pharmaceuticals during the identification tests.
• Quantitative analysis: Quantitative analysis is one of the fundamental aspects of pharmaceutical analysis. Our quantitative analysis ensures that the drugs are correctly formulated and that the levels of impurities are within acceptable limits to guarantee product safety and efficacy. We determine the content and purity of various components in a drug, including:
  
  • Active ingredients analysis
  • Excipient analysis
  • Impurities analysis
  • Related substance analysis
  • Heavy metals analysis
  • Moisture content analysis
• Physical property analysis: Besides, we analyze the physical properties of pharmaceuticals, another important component of pharmaceutical analysis. It encompasses the evaluation of various physical characteristics of drugs, such as solubility, particle size and shape, crystalline structure, and melting point. These properties directly influence drug stability, bioavailability, and manufacturing processes.
• Microbiological analysis: We also perform microbiological testing on pharmaceuticals, including the detection of microorganisms like Escherichia coli. This aspect of pharmaceutical analysis allows us to assess the microbial profile of the medications and ensure their safety and efficacy. By conducting such tests, we can identify any potential contamination.
• Bioavailability analysis: Our research revolves around comprehending the processes of drug absorption, distribution, metabolism, and excretion within the human body. These studies provide essential information to assess the pharmaceutical's effectiveness and determine the appropriate dosage regimen. We perform various assays to assess the bioavailability of pharmaceuticals, including evaluating aqueous solubility in simulated fluids, measuring drug absorption in the intestines, investigating interactions with transporters, and conducting protein binding assays. There is a wide range of animal models to choose from for research purposes and they can be ordered individually or combined at CD BioGlyco.
• Toxicology evaluation: Our service also involves studying the potential toxicity and adverse effects of drugs. It includes assessing acute and chronic toxicity, as well as evaluating the genotoxicity (potential for DNA damage) and carcinogenicity (potential to cause cancer) of drugs.
• Drug interaction analysis: We conduct drug interaction studies to explore the potential interactions between drugs and other substances, such as food, beverages, or other medications. These studies are crucial for identifying any possible drug-drug interactions or drug-food interactions that could impact the safety and effectiveness of the drugs.
• Stability analysis: In addition, we examine the stability characteristics of drugs under different storage conditions. These studies aim to establish appropriate storage requirements, expiry dates, and recommended handling procedures for pharmaceutical products, ensuring their safety and efficacy over their intended shelf life.
• Other analysis
  
  • Clarity and color of the solution
  • PH value
  • Loss on drying

Publication Data

Advantages

• We have built an extensive database of pharmaceutical compounds, their properties, and analytical methods. This database serves as a valuable resource for quick reference and comparison during the analysis process. It enables us to efficiently identify and quantify analytes, saving both time and effort.
• Our team excels in developing and optimizing analytical methods for pharmaceutical analysis. We understand the importance of achieving accurate, sensitive, and selective measurements. Through method development and optimization, we enhance the efficiency and effectiveness of our analysis, resulting in reliable and precise results.
• We have expertise in conducting stability studies for pharmaceutical products. These studies assess the integrity and shelf life of drugs under different storage conditions. By monitoring degradation and impurities over time, we can provide valuable information about product stability, aiding in formulation and manufacturing decisions.

CD BioGlyco offers unparalleled pharmaceutical analysis services with our advanced techniques. We possess a research team consisting of experienced professionals with extensive expertise in the field. They are equipped with advanced technology and knowledge to handle a wide range of analysis needs for pharmaceuticals, biologicals, and Pharmaceutical Excipients. With our state-of-the-art methodologies, we are committed to delivering accurate and reliable results. We ensure the highest level of accuracy and reliability in our analyses and our staff undergoes continuous training and development to stay updated with the latest advancements in pharmaceutical analysis. Partnering with CD BioGlyco for your pharmaceutical analysis needs ensures that you receive top-notch service and actionable insights. Our team is dedicated to helping you make informed decisions and advance your drug development process. Contact us today to learn more about how we can assist you in achieving your analytical goals.